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1.
Cornea ; 29(7): 807-11, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20489598

ABSTRACT

PURPOSE: This study evaluates the in vitro stability and sterility of fortified ophthalmic antibiotic preparations of 5% solutions (50 mg/mL) made from commercially available powders of amikacin, ceftazidime, and vancomycin stored at -20 degrees C for 6 months. METHODS: Antibiotic solutions were prepared with aseptic techniques by reconstitution and dilution of the commercially available powders (amikacin, ceftazidime, and vancomycin) and stored at -20 degrees C. After various durations of storage, the stability of various physical and chemical properties was determined by a pH meter, an osmometer, and high-performance liquid chromatography. Microbiological activity was assayed according to the European Pharmacopoeia. RESULTS: Solutions of 5% amikacin or ceftazidime in 0.9% sodium chloride and vancomycin in 5% dextrose were found to be physically, chemically, and microbiologically stable after storage at -20 degrees C for 190 days. A time limitation of 6 months is proposed. CONCLUSION: Fortified ophthalmic antibiotic solutions prepared and supplied by a pharmacy can be stored in freezers at -20 degrees C for later use.


Subject(s)
Anti-Bacterial Agents/chemistry , Drug Stability , Drug Storage , Ophthalmic Solutions/chemistry , Amikacin/chemistry , Ceftazidime/chemistry , Cryopreservation , Microbial Sensitivity Tests , Time Factors , Vancomycin/chemistry
2.
Therapie ; 60(5): 499-505, 2005.
Article in French | MEDLINE | ID: mdl-16433016

ABSTRACT

BACKGROUND: Administration of cisplatin requires hyperhydration of the patient to prevent nephrotoxic effects of this molecule. MATERIALS AND METHODS: A survey done in different hospitals - university hospitals, general hospitals and cancer institutes--has shown a large variability in the hydration protocols. A multidisciplinary group was set up in our university hospital comprising oncologists, nephrologists and pharmacists. This group has developed a consensual local protocol from a bibliographic analysis (Medline) and from the personal experience of each member. CONCLUSION: This protocol was approved by our hospital's Committee of Drugs and Medical Devices.


Subject(s)
Cisplatin/adverse effects , Fluid Therapy/methods , Neoplasms/drug therapy , Cisplatin/therapeutic use , Clinical Trials as Topic , Humans , Solutions
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